Safety, tolerability, pharmacokinetics, and pharmacodynamics of GLPG1690, a novel autotaxin inhibitor, to treat idiopathic pulmonary fibrosis (FLORA): a phase 2a …

TM Maher, EM van der Aar, O Van de Steen… - The Lancet …, 2018 - thelancet.com
Background Idiopathic pulmonary fibrosis (IPF) causes irreversible loss of lung function.
People with IPF have increased concentrations of autotaxin in lung tissue and …

Rationale, design and objectives of two phase III, randomised, placebo-controlled studies of GLPG1690, a novel autotaxin inhibitor, in idiopathic pulmonary fibrosis …

TM Maher, M Kreuter, DJ Lederer… - BMJ open …, 2019 - bmjopenrespres.bmj.com
Introduction While current standard of care (SOC) for idiopathic pulmonary fibrosis (IPF)
slows disease progression, prognosis remains poor. Therefore, an unmet need exists for …

Ziritaxestat, a novel autotaxin inhibitor, and lung function in idiopathic pulmonary fibrosis: the ISABELA 1 and 2 randomized clinical trials

TM Maher, P Ford, KK Brown, U Costabel, V Cottin… - Jama, 2023 - jamanetwork.com
Importance There is a major need for effective, well-tolerated treatments for idiopathic
pulmonary fibrosis (IPF). Objective To assess the efficacy and safety of the autotaxin inhibitor …

Discovery of 2-[[2-Ethyl-6-[4-[2-(3-hydroxyazetidin-1-yl)-2-oxoethyl]piperazin-1-yl]-8-methylimidazo[1,2-a]pyridin-3-yl]methylamino]-4-(4-fluorophenyl)thiazole-5 …

N Desroy, C Housseman, X Bock, A Joncour… - 2017 - ACS Publications
Autotaxin is a circulating enzyme with a major role in the production of lysophosphatic acid
(LPA) species in blood. A role for the autotaxin/LPA axis has been suggested in many …

Novel autotaxin inhibitor for the treatment of idiopathic pulmonary fibrosis: a clinical candidate discovered using DNA-encoded chemistry

JW Cuozzo, MA Clark, AD Keefe… - Journal of Medicinal …, 2020 - ACS Publications
The activity of the secreted phosphodiesterase autotaxin produces the inflammatory
signaling molecule LPA and has been associated with a number of human diseases …

Target inhibition of galectin-3 by inhaled TD139 in patients with idiopathic pulmonary fibrosis

N Hirani, AC MacKinnon, L Nicol, P Ford… - European …, 2021 - Eur Respiratory Soc
Galectin (Gal)-3 is a profibrotic β-galactoside-binding lectin that plays a key role in the
pathogenesis of idiopathic pulmonary fibrosis (IPF) and IPF exacerbations. TD139 is a novel …

A phase 2 randomized controlled study of tralokinumab in subjects with idiopathic pulmonary fibrosis

JM Parker, IN Glaspole, LH Lancaster… - American journal of …, 2018 - atsjournals.org
Rationale: IL-13 is a potential therapeutic target for idiopathic pulmonary fibrosis (IPF);
preclinical data suggest a role in tissue fibrosis, and expression is increased in subjects with …

[HTML][HTML] Pharmacotherapy and adjunctive treatment for idiopathic pulmonary fibrosis (IPF)

S Saito, A Alkhatib, JK Kolls, Y Kondoh… - Journal of thoracic …, 2019 - ncbi.nlm.nih.gov
Idiopathic pulmonary fibrosis (IPF) is an advancing and fatal lung disease with increasing
incidence and prevalence. Nintedanib and pirfenidone were approved by the FDA for the …

Effect of recombinant human pentraxin 2 vs placebo on change in forced vital capacity in patients with idiopathic pulmonary fibrosis: a randomized clinical trial

G Raghu, B Van Den Blink, MJ Hamblin, AW Brown… - Jama, 2018 - jamanetwork.com
Importance Idiopathic pulmonary fibrosis (IPF) is a progressive fibrotic lung disease with
poor prognosis. Approved therapies do not halt disease progression. Objective To …

Long-term treatment with recombinant human pentraxin 2 protein in patients with idiopathic pulmonary fibrosis: an open-label extension study

G Raghu, B van den Blink, MJ Hamblin… - The Lancet …, 2019 - thelancet.com
Background Patients with idiopathic pulmonary fibrosis (IPF) treated with PRM-151, a
recombinant human pentraxin 2 protein, in a phase 2 double-blind, randomised controlled …